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Measures

Number of red blood cells in the blood

Identifies

Red blood cell disorders

Measures: Number of red blood cells in the blood

Identifies: Red blood cell disorders

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What is the maximum days the report can be obtained for the test

The maximum days the report can be obtained for the test Congenital Hepatic Fibrosis (CHF) Gene Panel is 14 days.

What are the prerequisites for the test Congenital Hepatic Fibrosis (CHF) Gene Panel

  • Requisition form completely filled out with patient information
  • Consent form signed by patient or legal guardian
  • Specimen requirements: 2-5 mL blood in EDTA tube
  • Shipping requirements: Ship overnight on ice packs
  • Turnaround time: 3-4 weeks

What are the measure values for the test Congenital Hepatic Fibrosis (CHF) Gene Panel

  • Gene Panel: Congenital Hepatic Fibrosis (CHF)
  • Number of Genes: 9
  • Number of Variants: 112
  • Test Type: Genetic Testing
  • Sample Type: Blood or Saliva

What does this test Congenital Hepatic Fibrosis (CHF) Gene Panel identify?

  • The Congenital Hepatic Fibrosis (CHF) Gene Panel is a genetic test that identifies mutations in genes associated with congenital hepatic fibrosis, a rare genetic disorder characterized by the development of fibrosis in the liver and the presence of abnormal bile ducts.
  • This test specifically looks for mutations in genes such as PKHD1, which is the most commonly associated gene with CHF, as well as other genes like HNF1B and PKD1 that have been linked to the development of this condition.
  • Identifying these mutations can help confirm a diagnosis of congenital hepatic fibrosis and provide important information for genetic counseling and family planning.
  • Additionally, knowing the specific genetic mutations can also help guide treatment and management strategies for individuals with CHF.

Why is this test Congenital Hepatic Fibrosis (CHF) Gene Panel taken?

Test Name: Congenital Hepatic Fibrosis (CHF) Gene Panel

Reason for Test:

  • Congenital Hepatic Fibrosis (CHF) is a rare genetic disorder characterized by fibrosis and cystic dilatation of the intrahepatic bile ducts.
  • The CHF Gene Panel test is taken to identify mutations in genes associated with CHF, helping in the diagnosis and management of the condition.
  • Early detection of genetic mutations can enable timely intervention and appropriate treatment to improve outcomes for individuals with CHF.

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